posted on 2018-01-12, 00:00authored byErik Wetterskog, Christian Jonasson, Detlef-M. Smilgies, Vincent Schaller, Christer Johansson, Peter Svedlindh
One of the ultimate
goals of nanocrystal self-assembly is to transform
nanoscale building blocks into a material that displays enhanced properties
relative to the sum of its parts. Herein, we demonstrate that 1D needle-shaped
assemblies composed of Fe3−δO4 nanocubes
display a significant augmentation of the magnetic susceptibility
and dissipation as compared to 0D and 2D systems. The performance
of the nanocube needles is highlighted by a colossal anisotropy factor
defined as the ratio of the parallel to the perpendicular magnetization
components. We show that the origin of this effect cannot be ascribed
to shape anisotropy in its classical sense; as such, it has no analogy
in bulk magnetic materials. The temperature-dependent anisotropy factors
of the in- and out-of-phase components of the magnetization have an
extremely strong particle size dependence and reach values of 80 and
2500, respectively, for the largest nanocubes in this study. Aided
by simulations, we ascribe the anisotropy of the magnetic susceptibility,
and its strong particle-size dependence to a synergistic coupling
between the dipolar interaction field and a net anisotropy field resulting
from a partial texture in the 1D nanocube needles.